Corvò R, Vitale V, Barra S, Bacigalupo A, Locatelli F, Van Lint M T
Istituto Nazionale per la Ricerca sul Cancro, Genova.
Radiol Med. 1991 Jan-Feb;81(1-2):150-5.
From April 1976 through August 1989, 66 patients with aplastic anemia were treated on either of two immunosuppressive regimens in preparation for allogeneic bone marrow transplantation (BMT) from matched donor. Seventeen patients were treated with cyclophosphamide (50 mg/kg for 3 days) followed by thoracoabdominal irradiation (TAI), 6 Gy/1 fr and 2 patients, receiving marrow graft from partially matched family donors, were treated with cyclophosphamide (50 mg/kg for 3 days), TAI (6 Gy/1 fr) and Ara-C (4 g/mq for 2 days). Forty-seven more patients were treated with cyclophosphamide alone (50 mg/kg for 4 days). All patients received prophylactic treatment with methotrexate (15) or cyclosporine A (51) to avoid graft-versus-host disease. Mean time to engraftment was 12 days after chemotherapy and TAI and 15 days after cyclophosphamide (Cy) alone. No marrow rejections were observed in the TAI group: the two infants that received partially matched marrow allografted and are alive and well. Two patients treated with cyclophosphamide alone rejected allogeneic marrow. Long-term overall survivals are similar: 64% for TAI + Cy group and 56% for Cy alone group. In spite of the immunosuppressive regimen employed, young patients (under 20 years) do better than older ones (survival: 65% vs 45%, respectively). Thus, patient's age seems to be the main factor determining overall survival after allogeneic BMT. We conclude that the use of irradiation does not add significantly to the survival of aplastic patients; given the possible toxic long-term effects of irradiation, it would probably be wise to restrict the combined use of cyclophosphamide and irradiation to the patients sensitized to their donors, to those receiving partially matched marrow from family donors or in programs involving T-cell depletion.
从1976年4月至1989年8月,66例再生障碍性贫血患者接受了两种免疫抑制方案中的一种治疗,为接受匹配供体的异基因骨髓移植(BMT)做准备。17例患者接受环磷酰胺(50mg/kg,连用3天),随后进行胸腹照射(TAI),6Gy/单次照射;2例接受部分匹配的家族供体骨髓移植的患者,接受环磷酰胺(50mg/kg,连用3天)、TAI(6Gy/单次照射)和阿糖胞苷(4g/m²,连用2天)治疗。另外47例患者仅接受环磷酰胺治疗(50mg/kg,连用4天)。所有患者均接受甲氨蝶呤(15例)或环孢素A(51例)预防性治疗,以避免移植物抗宿主病。化疗和TAI后平均植入时间为12天,单纯环磷酰胺(Cy)治疗后为15天。TAI组未观察到骨髓排斥反应:2例接受部分匹配骨髓移植的婴儿存活且状况良好。2例仅接受环磷酰胺治疗的患者排斥了异基因骨髓。长期总生存率相似:TAI+Cy组为64%,单纯Cy组为56%。尽管采用了免疫抑制方案,但年轻患者(20岁以下)的情况优于年长患者(生存率分别为65%和45%)。因此,患者年龄似乎是决定异基因BMT后总生存的主要因素。我们得出结论,照射的使用并未显著提高再生障碍性贫血患者的生存率;鉴于照射可能存在的长期毒性作用,将环磷酰胺与照射联合使用可能明智地限制于对供体敏感的患者、接受家族供体部分匹配骨髓的患者或涉及T细胞去除的方案中。